Convective diffusive mixing in concentration polarization: from Taylor dispersion to surface convection
We analyse the steady-state convection–diffusion mixing of a solute by a creeping circulatory flow in a long sealed rectangular two-dimensional channel with impermeable sidewalls and fixed different solute concentrations at the two opposite edges. Solution circulation is due to a constant velocity s...
Gespeichert in:
Veröffentlicht in: | Journal of fluid mechanics 2013-08, Vol.728, p.239-278 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 278 |
---|---|
container_issue | |
container_start_page | 239 |
container_title | Journal of fluid mechanics |
container_volume | 728 |
creator | Rubinstein, I. Zaltzman, B. |
description | We analyse the steady-state convection–diffusion mixing of a solute by a creeping circulatory flow in a long sealed rectangular two-dimensional channel with impermeable sidewalls and fixed different solute concentrations at the two opposite edges. Solution circulation is due to a constant velocity slip along the sidewalls and a back flow along the channel axis. This simple model distils the essence of circulation in concentration polarization of an electrolyte solution under a DC electric current in a micro-channel sealed by an ion-selective element (a nano-channel or a cation exchange membrane). It is observed that in the slow circulation regime (small
$Pe$
numbers) the solute flux through the channel is governed by the Taylor–Aris dispersion mechanism, i.e. the flux is driven by the cross-sectional average axial concentration gradient, whereas upon increase in
$Pe$
this mechanism fails. The general question addressed is where the system goes after the breakdown of the Taylor–Aris dispersion regime. In order to find out the answer, the following specific questions have to be addressed. (1) How does the Taylor–Aris dispersion mechanism break down upon increase in
$Pe$
? (2) Why does it break down? (3) What is the role of the channel aspect ratio in this breakdown? The answers to these questions are obtained through analysing a hierarchy of suitable auxiliary model problems, including the unidirectional zero discharge channel flow and the circulatory analogue of plane-parallel Couette flow, for which most of the analysis is done. They may be summarized as follows. Upon increase in circulation velocity, the Taylor–Aris dispersion mechanism fails due to the formation of lateral non-uniformities of longitudinal solute concentration gradient driving the dispersion flux. These non-uniformities accumulate in protrusion-like disturbances of the solute concentration (wall fingers) emerging near the channel sidewall at the flow exit from the edge. Wall fingers propagate along the sidewalls with increase in
$Pe$
and eventually reach the opposite channel edges, transforming into narrow surface convection layers. These layers, together with the edge diffusion layers, form a closed mass transport pattern carrying most of the mass flux through the channel with the bulk largely excluded from the transport. The formation of this pattern finalizes the transition from Taylor–Aris dispersion to the surface convection regime. For large circulation velocities, concentration dis |
doi_str_mv | 10.1017/jfm.2013.276 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1710619154</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cupid>10_1017_jfm_2013_276</cupid><sourcerecordid>3802042711</sourcerecordid><originalsourceid>FETCH-LOGICAL-c369t-7f11b45751a9c223b768dd1c980a484c0d938e8e4fca3f374202cbcc06704e123</originalsourceid><addsrcrecordid>eNptkE1LxDAQhoMouK7e_AEF8WZrJk2b1pssfsGCl_Vc0jRZsrRJTdrF9deb7i7iwdPMwPM-Ay9C14ATwMDuN6pLCIY0ISw_QTOgeRmznGanaIYxITEAwefowvsNDhQu2QytF9ZspRj0VkaNVmr009bpL23WkTaRsEZIMzg-aGui3rbc6e_98RApZ7toxXetdSHre-n8BA028qNTXMgpvZdbc4nOFG-9vDrOOfp4flotXuPl-8vb4nEZizQvh5gpgJpmLANeCkLSmuVF04AoC8xpQQVuyrSQhaRK8FSljBJMRC0EzhmmEkg6RzcHb-_s5yj9UG3s6Ex4WQEDnEMJGQ3U3YESznrvpKp6pzvudhXgaqqyClVWU5VVqDLgt0cp94K3ynEjtP_NBISwMp20yVHLu9rpZi3_fP9P_ANahYSM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1710619154</pqid></control><display><type>article</type><title>Convective diffusive mixing in concentration polarization: from Taylor dispersion to surface convection</title><source>Cambridge University Press Journals</source><creator>Rubinstein, I. ; Zaltzman, B.</creator><creatorcontrib>Rubinstein, I. ; Zaltzman, B.</creatorcontrib><description>We analyse the steady-state convection–diffusion mixing of a solute by a creeping circulatory flow in a long sealed rectangular two-dimensional channel with impermeable sidewalls and fixed different solute concentrations at the two opposite edges. Solution circulation is due to a constant velocity slip along the sidewalls and a back flow along the channel axis. This simple model distils the essence of circulation in concentration polarization of an electrolyte solution under a DC electric current in a micro-channel sealed by an ion-selective element (a nano-channel or a cation exchange membrane). It is observed that in the slow circulation regime (small
$Pe$
numbers) the solute flux through the channel is governed by the Taylor–Aris dispersion mechanism, i.e. the flux is driven by the cross-sectional average axial concentration gradient, whereas upon increase in
$Pe$
this mechanism fails. The general question addressed is where the system goes after the breakdown of the Taylor–Aris dispersion regime. In order to find out the answer, the following specific questions have to be addressed. (1) How does the Taylor–Aris dispersion mechanism break down upon increase in
$Pe$
? (2) Why does it break down? (3) What is the role of the channel aspect ratio in this breakdown? The answers to these questions are obtained through analysing a hierarchy of suitable auxiliary model problems, including the unidirectional zero discharge channel flow and the circulatory analogue of plane-parallel Couette flow, for which most of the analysis is done. They may be summarized as follows. Upon increase in circulation velocity, the Taylor–Aris dispersion mechanism fails due to the formation of lateral non-uniformities of longitudinal solute concentration gradient driving the dispersion flux. These non-uniformities accumulate in protrusion-like disturbances of the solute concentration (wall fingers) emerging near the channel sidewall at the flow exit from the edge. Wall fingers propagate along the sidewalls with increase in
$Pe$
and eventually reach the opposite channel edges, transforming into narrow surface convection layers. These layers, together with the edge diffusion layers, form a closed mass transport pattern carrying most of the mass flux through the channel with the bulk largely excluded from the transport. The formation of this pattern finalizes the transition from Taylor–Aris dispersion to the surface convection regime. For large circulation velocities, concentration distribution in the surface convection layers attains an oscillatory spiral structure reminiscent of thermal waves in heat conduction.</description><identifier>ISSN: 0022-1120</identifier><identifier>EISSN: 1469-7645</identifier><identifier>DOI: 10.1017/jfm.2013.276</identifier><identifier>CODEN: JFLSA7</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Applied fluid mechanics ; Atmospheric circulation ; Cation exchange ; Channel flow ; Convection ; Diffusion ; Dispersion ; Exact sciences and technology ; Fluctuations ; Fluid dynamics ; Fluidics ; Fundamental areas of phenomenology (including applications) ; Mass transport ; Physics ; Zero discharge</subject><ispartof>Journal of fluid mechanics, 2013-08, Vol.728, p.239-278</ispartof><rights>2013 Cambridge University Press</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-7f11b45751a9c223b768dd1c980a484c0d938e8e4fca3f374202cbcc06704e123</citedby><cites>FETCH-LOGICAL-c369t-7f11b45751a9c223b768dd1c980a484c0d938e8e4fca3f374202cbcc06704e123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0022112013002760/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>164,314,780,784,27924,27925,55628</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27627934$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Rubinstein, I.</creatorcontrib><creatorcontrib>Zaltzman, B.</creatorcontrib><title>Convective diffusive mixing in concentration polarization: from Taylor dispersion to surface convection</title><title>Journal of fluid mechanics</title><addtitle>J. Fluid Mech</addtitle><description>We analyse the steady-state convection–diffusion mixing of a solute by a creeping circulatory flow in a long sealed rectangular two-dimensional channel with impermeable sidewalls and fixed different solute concentrations at the two opposite edges. Solution circulation is due to a constant velocity slip along the sidewalls and a back flow along the channel axis. This simple model distils the essence of circulation in concentration polarization of an electrolyte solution under a DC electric current in a micro-channel sealed by an ion-selective element (a nano-channel or a cation exchange membrane). It is observed that in the slow circulation regime (small
$Pe$
numbers) the solute flux through the channel is governed by the Taylor–Aris dispersion mechanism, i.e. the flux is driven by the cross-sectional average axial concentration gradient, whereas upon increase in
$Pe$
this mechanism fails. The general question addressed is where the system goes after the breakdown of the Taylor–Aris dispersion regime. In order to find out the answer, the following specific questions have to be addressed. (1) How does the Taylor–Aris dispersion mechanism break down upon increase in
$Pe$
? (2) Why does it break down? (3) What is the role of the channel aspect ratio in this breakdown? The answers to these questions are obtained through analysing a hierarchy of suitable auxiliary model problems, including the unidirectional zero discharge channel flow and the circulatory analogue of plane-parallel Couette flow, for which most of the analysis is done. They may be summarized as follows. Upon increase in circulation velocity, the Taylor–Aris dispersion mechanism fails due to the formation of lateral non-uniformities of longitudinal solute concentration gradient driving the dispersion flux. These non-uniformities accumulate in protrusion-like disturbances of the solute concentration (wall fingers) emerging near the channel sidewall at the flow exit from the edge. Wall fingers propagate along the sidewalls with increase in
$Pe$
and eventually reach the opposite channel edges, transforming into narrow surface convection layers. These layers, together with the edge diffusion layers, form a closed mass transport pattern carrying most of the mass flux through the channel with the bulk largely excluded from the transport. The formation of this pattern finalizes the transition from Taylor–Aris dispersion to the surface convection regime. For large circulation velocities, concentration distribution in the surface convection layers attains an oscillatory spiral structure reminiscent of thermal waves in heat conduction.</description><subject>Applied fluid mechanics</subject><subject>Atmospheric circulation</subject><subject>Cation exchange</subject><subject>Channel flow</subject><subject>Convection</subject><subject>Diffusion</subject><subject>Dispersion</subject><subject>Exact sciences and technology</subject><subject>Fluctuations</subject><subject>Fluid dynamics</subject><subject>Fluidics</subject><subject>Fundamental areas of phenomenology (including applications)</subject><subject>Mass transport</subject><subject>Physics</subject><subject>Zero discharge</subject><issn>0022-1120</issn><issn>1469-7645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkE1LxDAQhoMouK7e_AEF8WZrJk2b1pssfsGCl_Vc0jRZsrRJTdrF9deb7i7iwdPMwPM-Ay9C14ATwMDuN6pLCIY0ISw_QTOgeRmznGanaIYxITEAwefowvsNDhQu2QytF9ZspRj0VkaNVmr009bpL23WkTaRsEZIMzg-aGui3rbc6e_98RApZ7toxXetdSHre-n8BA028qNTXMgpvZdbc4nOFG-9vDrOOfp4flotXuPl-8vb4nEZizQvh5gpgJpmLANeCkLSmuVF04AoC8xpQQVuyrSQhaRK8FSljBJMRC0EzhmmEkg6RzcHb-_s5yj9UG3s6Ex4WQEDnEMJGQ3U3YESznrvpKp6pzvudhXgaqqyClVWU5VVqDLgt0cp94K3ynEjtP_NBISwMp20yVHLu9rpZi3_fP9P_ANahYSM</recordid><startdate>20130810</startdate><enddate>20130810</enddate><creator>Rubinstein, I.</creator><creator>Zaltzman, B.</creator><general>Cambridge University Press</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TB</scope><scope>7U5</scope><scope>7UA</scope><scope>7XB</scope><scope>88I</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H8D</scope><scope>H96</scope><scope>HCIFZ</scope><scope>KR7</scope><scope>L.G</scope><scope>L6V</scope><scope>L7M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>S0W</scope></search><sort><creationdate>20130810</creationdate><title>Convective diffusive mixing in concentration polarization: from Taylor dispersion to surface convection</title><author>Rubinstein, I. ; Zaltzman, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-7f11b45751a9c223b768dd1c980a484c0d938e8e4fca3f374202cbcc06704e123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Applied fluid mechanics</topic><topic>Atmospheric circulation</topic><topic>Cation exchange</topic><topic>Channel flow</topic><topic>Convection</topic><topic>Diffusion</topic><topic>Dispersion</topic><topic>Exact sciences and technology</topic><topic>Fluctuations</topic><topic>Fluid dynamics</topic><topic>Fluidics</topic><topic>Fundamental areas of phenomenology (including applications)</topic><topic>Mass transport</topic><topic>Physics</topic><topic>Zero discharge</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rubinstein, I.</creatorcontrib><creatorcontrib>Zaltzman, B.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Water Resources Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Aerospace Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>SciTech Premium Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>ProQuest Engineering Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest research library</collection><collection>Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>DELNET Engineering & Technology Collection</collection><jtitle>Journal of fluid mechanics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rubinstein, I.</au><au>Zaltzman, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Convective diffusive mixing in concentration polarization: from Taylor dispersion to surface convection</atitle><jtitle>Journal of fluid mechanics</jtitle><addtitle>J. Fluid Mech</addtitle><date>2013-08-10</date><risdate>2013</risdate><volume>728</volume><spage>239</spage><epage>278</epage><pages>239-278</pages><issn>0022-1120</issn><eissn>1469-7645</eissn><coden>JFLSA7</coden><abstract>We analyse the steady-state convection–diffusion mixing of a solute by a creeping circulatory flow in a long sealed rectangular two-dimensional channel with impermeable sidewalls and fixed different solute concentrations at the two opposite edges. Solution circulation is due to a constant velocity slip along the sidewalls and a back flow along the channel axis. This simple model distils the essence of circulation in concentration polarization of an electrolyte solution under a DC electric current in a micro-channel sealed by an ion-selective element (a nano-channel or a cation exchange membrane). It is observed that in the slow circulation regime (small
$Pe$
numbers) the solute flux through the channel is governed by the Taylor–Aris dispersion mechanism, i.e. the flux is driven by the cross-sectional average axial concentration gradient, whereas upon increase in
$Pe$
this mechanism fails. The general question addressed is where the system goes after the breakdown of the Taylor–Aris dispersion regime. In order to find out the answer, the following specific questions have to be addressed. (1) How does the Taylor–Aris dispersion mechanism break down upon increase in
$Pe$
? (2) Why does it break down? (3) What is the role of the channel aspect ratio in this breakdown? The answers to these questions are obtained through analysing a hierarchy of suitable auxiliary model problems, including the unidirectional zero discharge channel flow and the circulatory analogue of plane-parallel Couette flow, for which most of the analysis is done. They may be summarized as follows. Upon increase in circulation velocity, the Taylor–Aris dispersion mechanism fails due to the formation of lateral non-uniformities of longitudinal solute concentration gradient driving the dispersion flux. These non-uniformities accumulate in protrusion-like disturbances of the solute concentration (wall fingers) emerging near the channel sidewall at the flow exit from the edge. Wall fingers propagate along the sidewalls with increase in
$Pe$
and eventually reach the opposite channel edges, transforming into narrow surface convection layers. These layers, together with the edge diffusion layers, form a closed mass transport pattern carrying most of the mass flux through the channel with the bulk largely excluded from the transport. The formation of this pattern finalizes the transition from Taylor–Aris dispersion to the surface convection regime. For large circulation velocities, concentration distribution in the surface convection layers attains an oscillatory spiral structure reminiscent of thermal waves in heat conduction.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><doi>10.1017/jfm.2013.276</doi><tpages>40</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1120 |
ispartof | Journal of fluid mechanics, 2013-08, Vol.728, p.239-278 |
issn | 0022-1120 1469-7645 |
language | eng |
recordid | cdi_proquest_journals_1710619154 |
source | Cambridge University Press Journals |
subjects | Applied fluid mechanics Atmospheric circulation Cation exchange Channel flow Convection Diffusion Dispersion Exact sciences and technology Fluctuations Fluid dynamics Fluidics Fundamental areas of phenomenology (including applications) Mass transport Physics Zero discharge |
title | Convective diffusive mixing in concentration polarization: from Taylor dispersion to surface convection |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T00%3A58%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Convective%20diffusive%20mixing%20in%20concentration%20polarization:%20from%20Taylor%20dispersion%20to%20surface%20convection&rft.jtitle=Journal%20of%20fluid%20mechanics&rft.au=Rubinstein,%20I.&rft.date=2013-08-10&rft.volume=728&rft.spage=239&rft.epage=278&rft.pages=239-278&rft.issn=0022-1120&rft.eissn=1469-7645&rft.coden=JFLSA7&rft_id=info:doi/10.1017/jfm.2013.276&rft_dat=%3Cproquest_cross%3E3802042711%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1710619154&rft_id=info:pmid/&rft_cupid=10_1017_jfm_2013_276&rfr_iscdi=true |